Cleared Traditional

K984377 - SYNTHES SPINE CERVIFIX SYSTEM

K984377 is the FDA 510(k) clearance for SYNTHES SPINE CERVIFIX SYSTEM by Synthes (Usa). It is a Class 2 Orthopedic device (product code KWP) cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K984377 · Synthes (Usa) · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1999
Decision
49d
Days
Class 2
Risk

K984377 is an FDA 510(k) clearance for the SYNTHES SPINE CERVIFIX SYSTEM. Classified as Appliance, Fixation, Spinal Interlaminal (product code KWP), Class II - Special Controls.

Submitted by Synthes (Usa) (Paoli, US). The FDA issued a Cleared decision on January 21, 1999 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3050 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Synthes (Usa) devices

Submission Details

510(k) Number K984377 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 03, 1998
Decision Date January 21, 1999
Days to Decision 49 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 122d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KWP Appliance, Fixation, Spinal Interlaminal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3050
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - KWP Appliance, Fixation, Spinal Interlaminal

All 265
Devices cleared under the same product code (KWP) and FDA review panel - the closest regulatory comparables to K984377.
OSTEONICS SPINAL SYSTEM - SACRAL OFFSET CONNECTOR ASSEMBLY
K984375 · Osteonics Corp. · Apr 1999
TITANIUM VERSALOK
K990708 · Wrightmedicaltechnologyinc · Mar 1999
CD HORIZON SPINAL SYSTEM
K981676 · Sofamor Danek USA,Inc. · Jan 1999
ROGOZINSKI SPINAL ROD SYSTEM
K983904 · United States Surgical, A Division of Tyco Healthc · Dec 1998
SYNTHES POSTERIOR UNIVERSAL SPINAL SYSTEM
K983530 · Synthes (Usa) · Dec 1998
DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS
K983583 · Depuy, Inc. · Dec 1998